@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP74657.RAMh3G5TDxtCDQG7RX-_uaY8U9hf0QibSna2VeBhLBwaQ
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP74657.RAMh3G5TDxtCDQG7RX-_uaY8U9hf0QibSna2VeBhLBwaQ130_head
{
this:
np:hasAssertion
dgn-np:NP74657.RAMh3G5TDxtCDQG7RX-_uaY8U9hf0QibSna2VeBhLBwaQ130_assertion
;
np:hasProvenance
dgn-np:NP74657.RAMh3G5TDxtCDQG7RX-_uaY8U9hf0QibSna2VeBhLBwaQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP74657.RAMh3G5TDxtCDQG7RX-_uaY8U9hf0QibSna2VeBhLBwaQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP74657.RAMh3G5TDxtCDQG7RX-_uaY8U9hf0QibSna2VeBhLBwaQ130_assertion
a
np:Assertion
.
dgn-np:NP74657.RAMh3G5TDxtCDQG7RX-_uaY8U9hf0QibSna2VeBhLBwaQ130_provenance
a
np:Provenance
.
dgn-np:NP74657.RAMh3G5TDxtCDQG7RX-_uaY8U9hf0QibSna2VeBhLBwaQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP74657.RAMh3G5TDxtCDQG7RX-_uaY8U9hf0QibSna2VeBhLBwaQ130_assertion
{
miriam-gene:2539
a
ncit:C16612
.
lld:C0020435
a
ncit:C7057
.
dgn-gda:DGN14d4aa8bebd1f6d2a3bb7e2bd0d9abbf
sio:SIO_000628
miriam-gene:2539
,
lld:C0020435
;
a
sio:SIO_001122
.
}
dgn-np:NP74657.RAMh3G5TDxtCDQG7RX-_uaY8U9hf0QibSna2VeBhLBwaQ130_provenance
{
dgn-np:NP74657.RAMh3G5TDxtCDQG7RX-_uaY8U9hf0QibSna2VeBhLBwaQ130_assertion
dcterms:description
"[this expanded panel of mutations and polymorphisms can serve as an effective instrument to study the genetic architecture of hyperbilirubinemia and speculate an important role for genetic polymorphism coinheritance in determining hyperbilirubinemia risk i]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:18558634
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP74657.RAMh3G5TDxtCDQG7RX-_uaY8U9hf0QibSna2VeBhLBwaQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:36+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}